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Sahoko Miyama

Showing results (31-40 of 36) with videos related to

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Journal of Human Genetics|February 16, 2019
Nonsense variants in STAG2 result in distinct sex-dependent phenotypesHiromi Aoi, Ming Lei, Takeshi Mizuguchi, et al.
Human Genome Variation|October 5, 2020
Nonsense variants of <i>STAG2</i> result in distinct congenital anomaliesHiromi Aoi, Ming Lei, Takeshi Mizuguchi, et al.
Journal of Human Genetics|June 16, 2020
Retraction Note to: Nonsense variants in STAG2 result in distinct sex-dependent phenotypesHiromi Aoi, Ming Lei, Takeshi Mizuguchi, et al.
Annals of Neurology|January 26, 2012
Increased gene dosage of myelin protein zero causes Charcot-Marie-Tooth diseaseMeiko Hashimoto Maeda, Jun Mitsui, Bing-Wen Soong, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 21, 2024
Evidence-based diagnostic prediction score for pediatric NMDA receptor encephalitisShimpei Matsuda, Takayuki Mori, Mariko Kasai, et al.
Epilepsia|October 5, 2010
STXBP1 mutations in early infantile epileptic encephalopathy with suppression-burst patternHirotomo Saitsu, Mitsuhiro Kato, Ippei Okada, et al.
Pageof 4

Showing results (31-40 of 36) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 36 results.
Journal of Human Genetics|February 16, 2019
Nonsense variants in STAG2 result in distinct sex-dependent phenotypesHiromi Aoi, Ming Lei, Takeshi Mizuguchi, et al.
Human Genome Variation|October 5, 2020
Nonsense variants of <i>STAG2</i> result in distinct congenital anomaliesHiromi Aoi, Ming Lei, Takeshi Mizuguchi, et al.
Journal of Human Genetics|June 16, 2020
Retraction Note to: Nonsense variants in STAG2 result in distinct sex-dependent phenotypesHiromi Aoi, Ming Lei, Takeshi Mizuguchi, et al.
Annals of Neurology|January 26, 2012
Increased gene dosage of myelin protein zero causes Charcot-Marie-Tooth diseaseMeiko Hashimoto Maeda, Jun Mitsui, Bing-Wen Soong, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 21, 2024
Evidence-based diagnostic prediction score for pediatric NMDA receptor encephalitisShimpei Matsuda, Takayuki Mori, Mariko Kasai, et al.
Epilepsia|October 5, 2010
STXBP1 mutations in early infantile epileptic encephalopathy with suppression-burst patternHirotomo Saitsu, Mitsuhiro Kato, Ippei Okada, et al.
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